Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232543364T>A , CM000664.2:g.232543364T>A | GRCh38 |
| NC_000002.11:g.233408074T>A , CM000664.1:g.233408074T>A | GRCh37 |
| NC_000002.10:g.233116318T>A | NCBI36 |
| NG_012954.1:g.8638T>A | |
| NG_012954.2:g.8673T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005199.5:c.895T>A MANE Select | NP_005190.4:p.Ser299Thr |
| ENST00000651502.1:c.895T>A MANE Select | ENSP00000498757.1:p.Ser299Thr |
| NM_005199.4:c.895T>A | NP_005190.4:p.Ser299Thr |
| ENST00000389492.3:c.739T>A | ENSP00000374143.3:p.Ser247Thr |
| ENST00000389494.7:c.895T>A | ENSP00000374145.3:p.Ser299Thr |